ClinVar Miner

List of variants in gene combination LOC101927870, RELN reported as benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_005045.4(RELN):c.10093G>A (p.Val3365Ile) rs115035120
NM_005045.4(RELN):c.8508C>T (p.Phe2836=) rs2229862
NM_005045.4(RELN):c.8811G>A (p.Ala2937=) rs144728023
NM_005045.4(RELN):c.8944G>A (p.Asp2982Asn) rs148509350
NM_005045.4(RELN):c.9321C>T (p.Leu3107=) rs150387973
NM_005045.4(RELN):c.9370-13_9370-8del rs141397961
NM_005045.4(RELN):c.9524A>C (p.His3175Pro) rs74513461
NM_005045.4(RELN):c.9714C>T (p.His3238=) rs78218774
NM_005045.4(RELN):c.9730G>A (p.Gly3244Ser) rs73714410
NM_005045.4(RELN):c.9903C>T (p.Tyr3301=) rs73714404

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